Measuring Impact of Computer Gaming on Arm Use in Rett Syndrome

Rett Syndrome Clinical Trial

Official title:

Assessing the Effectiveness of Customized Computer Activities on Reducing Stereotypies and Improving Independent Upper Extremity Motor Skills in Persons With Rett Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05012475
• Other study ID #: 2015-0656
• Status: Recruiting
• Phase: N/A
• Start date: May 1, 2021
• Est. completion date: December 1, 2024

Study information

• Verified date: February 2023
• Source: Georgetown University
• Contact: Pamela S Diener, PhD, MS, OT/L
• Phone: 2403811763
• Email: psd23[@]georgetown.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Using a tele-research approach, we will recruit, enroll, guide and support carers and participants to engage in computer based activities (modified virtual reality) with the primary outcome of reducing stereotypies and increasing independent arm and hand use and secondary outcome of improving quality of living. Because of our virtual approach, we are able to recruit from multiple countries and all states and territories of the USA.

Description:

Early in life, individuals with Rett syndrome lose purposeful use of their hands and engage in handwringing and handmouthing stereotypies. It is important to pursue interventions that may facilitate the development and sustained use of arms/hands for productive involvement in daily needs that ultimately improve quality of life. Investigators plan to use a tele-research approach to assist caregivers and the participants in playing customized computer generated games that require independent and sustained hand separations and initiated and sustained movement patterns to control the modified virtual reality activity that serves as our intervention. Customization of the games and activities used will require collaboration with the caregivers of each participant to ensure that the level of motivation and interest of the participant matches the game/activities used. Brightly colored wristbands will be worn on each participant's wrist during the one-hour long intervention in which they will be involved 3 days per week for ~12 weeks. These wrist bands will be detected by the software we developed. As the participants move their arms, our software will detect these position changes and activate the computer-based activities. At 5 different points in the study investigators will test for changes in independent reaching abilities that may result from exposure to the intervention. Specifically, investigators will assess the impact of the intervention on minimizing hand stereotypies and improving the amount and quality of independent arm function. At the start and end of the study, investigators will also assess the impact the intervention had on activities of daily living, and therefore quality of life, via three goals developed in collaboration with the family/caregiver of the participant. Due to the virtual nature (tele-research) of the study, investigators aim to recruit 10-12 participants from multiple countries. Once enrolled, each participant will remain involved for up to 5-6 months. Since all activities are hand selected for each participant in collaboration with the caregivers, risks of involvement in this study are low. Investigators anticipate that this intervention will improve motor planning abilities for arm use and reduce stereotypies.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10
• Est. completion date: December 1, 2024
• Est. primary completion date: May 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years to 60 Years

Eligibility

Inclusion Criteria:

• Rett syndrome,

• Understanding of cause and effect,

• Functional range of motion of arms to complete the movements needed to control the games.

Exclusion Criteria:

• no competing orthopedic or neuromuscular diagnosis that impacts shoulder movements

Related Conditions & MeSH terms

• Rett Syndrome
• Syndrome

Intervention

Behavioral:
• Modified Virtual Reality Gaming
Investigators customize each gaming session based on the motivators and interests of each participant. The intervention facilitates independent hand separations (minimizing stereotypies) and encourages independent arm/hand movement that serves to activate or control the computer-generated activities.

Locations

Country	Name	City	State
United States	Georgetown University School of Medicine	Washington	District of Columbia

Sponsors (2)

Lead Sponsor	Collaborator
Georgetown University	International Rett Syndrome Foundation Rettsyndrome.org

Country where clinical trial is conducted

United States, 

References & Publications (3)

McAmis NE, Foreman MH, Himmelrich MD, Diener PS and Engsberg JR. Development of a Method to Use a Color Tracker for Motor Therapy for Individuals with Rett Syndrome. SM J Pediatr. 2017; 2(2): 1012.

Mraz KM, Amadio G, Diener P, Eisenberg G, Engsberg JR. Improving upper extremity motor skills in girls with rett syndrome using virtual reality. J of Intellect Disabil - Diagnosis and Treatment, 2016, 4(3):142-151.

Mraz, K, Eisenberg G, Diener P, Amadio G, Foreman MH, Engsberg JR. The Effects of Virtual Reality on the Upper Extremity Skills of Girls with Rett Syndrome: A Single Case Study. J of Intellect Disabil- Diagnosis and Treatment. 2016, 4(3):152-9.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	functional Reach Test	Investigators will video record all testing sessions so that the video can be viewed slow motion or frame by frame to count hand separations, number of reaches, time of sustained reaches, and sustained hand separations.	To measure change, this test is administered (repeated) 5 times during the 5 month study: Day 1 (baseline); Day 32 (start of wk long training); Day 40 (after one wk training session); Day Day 130 (end of 12 wk intervention); Day 160 (post-intervention).
Secondary	Goal Attainment Scale (GAS)	In collaboration with the parents/carers, investigators will create three goals specific for each participant that relate to study aims and improving quality of daily living.	To measure change, this test is administered on Day 1 (Baseline) and repeated at Day 120 (end of intervention phase)
Secondary	Functional Range of Motion (FROM)	Assess range of shoulder and hand motion at start and at end of study to be sure that shoulder mobility is unchanged and/or not impacting the required motions for the intervention.	To assess if a change in FROM occurs during the study, this test is administered on Day 1 (Baseline) and repeated at Day 120 (Post-intervention)